Canonical Allele Identifier: CA1845635789

Gene: GALT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34647247G= , CM000671.2:g.34647247G=	GRCh38
NC_000009.11:g.34647244G= , CM000671.1:g.34647244G=	GRCh37
NC_000009.10:g.34637244G=	NCBI36
NG_009029.1:g.5610G=
NG_028966.1:g.63G=
NG_009029.2:g.5659G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691183.1:c.241G=	ENSP00000509954.1:p.Ala81=
ENST00000378842.8:c.241G= MANE Select	ENSP00000368119.4:p.Ala81=
ENST00000378842.7:c.241G=	ENSP00000368119.3:p.Ala81=
ENST00000450095.6:c.39G=	ENSP00000401956.2:p.Glu13=
ENST00000465543.6:n.580G=
ENST00000468099.2:n.281G=
ENST00000472111.5:n.282G=
ENST00000473506.6:c.241G=	ENSP00000432839.2:p.Ala81=
ENST00000473529.5:n.288G=
ENST00000485531.1:n.234G=
ENST00000487381.5:n.267G=
ENST00000489643.6:n.271G=
ENST00000554085.5:c.241G=	ENSP00000450419.1:p.Ala81=
ENST00000554139.5:n.294G=
ENST00000554330.5:n.238G=
ENST00000554550.5:c.241G=	ENSP00000451435.1:p.Ala81=
ENST00000554638.5:n.265G=
ENST00000554897.5:c.241G=	ENSP00000450942.1:p.Ala81=
ENST00000554944.5:n.271G=
ENST00000555020.5:n.271G=
ENST00000555086.5:n.245G=
ENST00000555214.5:n.250G=
ENST00000556157.1:n.348G=
ENST00000556244.1:c.125G=
ENST00000556278.1:c.241G=	ENSP00000451792.1:p.Ala81=
ENST00000556403.5:n.254G=
ENST00000556494.5:n.273G=
ENST00000557541.5:n.434G=
ENST00000557706.5:n.355G=
NM_000155.3:c.241G=	NP_000146.2:p.Ala81=
NM_001258332.1:c.39G=	NP_001245261.1:p.Glu13=
NM_000155.4:c.241G= MANE Select	NP_000146.2:p.Ala81=
NM_001258332.2:c.39G=	NP_001245261.1:p.Glu13=